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Autori: Maver Ales

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Naslov Diagnostic and Clinical Utility of Clinical Exome Sequencing in Children With Moderate and Severe Global Developmental Delay / Intellectual Disability (Article)
Autori Ruml-Stojanovic Jelena Miletic Aleksandra Peterlin Borut Maver Ales Mijovic Marija Borlja Nikola Dimitrijevic Brankica Soldatovic Ivan A  Cuturilo Goran 
Info JOURNAL OF CHILD NEUROLOGY, (2020), vol. 35 br. 2, str. 116-131
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Clinical Next Generation Sequencing Reveals An H3f3a Gene as a New Potential Gene Candidate for Microcephaly Associated with Severe Developmental Delay, Intellectual Disability and Growth Retardation (Article)
Autori Maver Ales Cuturilo Goran Stojanovic Ruml J Peterlin Borut 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 22 br. 2, str. 65-68
Projekat Slovenian Research Agency - Slovenia [J3-8205, J3-9280, P3-0326]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Rare missense TUBGCP5 gene variant in a patient with primary microcephaly (Article)
Autori Maver Ales Cuturilo Goran Kovanda Anja Miletic Aleksandra Peterlin Borut 
Info EUROPEAN JOURNAL OF MEDICAL GENETICS, (2019), vol. 62 br. 12, str. -
Projekat ARRS research programme [P3-0326, J3-8205, J3-5506]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice (Article)
Autori Tumiene B Maver Ales Writzl Karin Hodzic A Cuturilo Goran Kuzmanic-Samija Radenka Culic V Peterlin Borut 
Info CLINICAL GENETICS, (2018), vol. 93 br. 5, str. 1057-1062
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases (Article)
Autori Bergant Gaber Maver Ales Lovrecic Luca Cuturilo Goran Hodzic Alenka Peterlin Borut 
Info GENETICS IN MEDICINE, (2018), vol. 20 br. 3, str. 303-312
Projekat Slovenian Research Agency [P3-0326]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis (Article)
Autori Maver Ales ... Drulovic Jelena S  Pekmezovic Tatjana D  Novakovic Ivana V  ... (broj koautora 19) 
Info SCIENTIFIC REPORTS, (2017), vol. 7 br. , str. -
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility (Article)
Autori Hodzic Alenka Ristanovic Momcilo Zorn Branko Tulic Cane Dz Maver Ales Novakovic Ivana V  Plaseska-Karanfilska D Peterlin Borut 
Info ANDROLOGY, (2017), vol. 5 br. 1, str. 70-74
Projekat Slovenian Research Agency [P3-0326]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility (Article)
Autori Hodzic Alenka Ristanovic Momcilo Zorn Branko Tulic Cane Dz Maver Ales Novakovic Ivana V  Peterlin Borut 
Info PLOS ONE, (2013), vol. 8 br. 3, str. -
Projekat National Research Agency of the Republic of Slovenia [P3-0326]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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